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Diisopropylethylamine → N-[{(2S)-4-(3,4-Dichlorobenzyl)morpholin-2-yl]methyl}-2-(5-phenyl-2H-tetraazol-2-yl)acetamide

HRID 2212013
ノート
印刷プレビュー

反応式

HRID 2212013 の反応式
[C:1]1([C:7]2[N:8]=[N:9][N:10]([CH2:12][C:13]([OH:15])=O)[N:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C(N(CC)C(C)C)(C)C.[Cl:25][C:26]1[CH:27]=[C:28]([CH:38]=[CH:39][C:40]=1[Cl:41])[CH2:29][N:30]1[CH2:35][CH2:34][O:33][C@@H:32]([CH2:36][NH2:37])[CH2:31]1>CN(C)C=O>[Cl:25][C:26]1[CH:27]=[C:28]([CH:38]=[CH:39][C:40]=1[Cl:41])[CH2:29][N:30]1[CH2:35][CH2:34][O:33][C@@H:32]([CH2:36][NH:37][C:13](=[O:15])[CH2:12][N:10]2[N:9]=[N:8][C:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)=[N:11]2)[CH2:31]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 81531DiisopropylethylamineHCID 10865632-(5-phenyl-2H-1,2,3,4-tetrazol-2-yl)acetic acidHCID 10171585(S)-(4-(3,4-Dichlorobenzyl)morpholin-2-YL)methanamine

生成物 1

HCID 68883559N-[{(2S)-4-(3,4-Dichlorobenzyl)morpholin-2-yl]methyl}-2-(5-phenyl-2H-tetraazol-2-yl)acetamide収率 99.8%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide
溶媒
2 回

反応条件

温度
22 °C

実験手順

A solution of (5-phenyl-2H-tetraazol-2-yl)acetic acid (0.082 g) in N,N-dimethylformamide (2 ml) under nitrogen was treated with O-(7-azabenzotriazol-1-yl)-N,N,N′N′-tetramethylammonium hexafluorophosphate (0.152 g) and N,N-diisopropylethylamine (0.139 ml) followed by a solution of Intermediate 9 (0.110 g) in N,N-dimethylformamide (3 ml), and the mixture was stirred at 22° C. for 4 h. The solvent was removed in vacuo and the residue dissolved in ethyl acetate (20 ml). The solution was washed with 10% aqueous citric acid (20 ml), brine (20 ml), saturated aqueous sodium hydrogen carbonate (20 ml) and brine (20 ml), dried (MgSO4) and evaporated in vacuo. Purification by flash chromatography on silica gel (Merck 9385), eluting with ethyl acetate, followed by trituration of the resultant product with diethyl ether, gave the title compound as a white solid (0.184 g).

後処理

  1. customThe solvent was removed in vacuo
  2. dissolutionthe residue dissolved in ethyl acetate (20 ml)
  3. washThe solution was washed with 10% aqueous citric acid (20 ml), brine (20 ml), saturated aqueous sodium hydrogen carbonate (20 ml) and brine (20 ml)
  4. dry with materialdried (MgSO4)
  5. customevaporated in vacuo
  6. customPurification by flash chromatography on silica gel (Merck 9385)
  7. washeluting with ethyl acetate

出典と根拠

ORDレコード
ord-d4ce371150474eae973372f60c85500e
出典データセット
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07101882B2

反応ノート

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